510(k) K211738

Device
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Applicant
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510(k) number
K211738
Product code
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Decision
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Decision date
2021-09-14
Date received
2021-06-07
Regulation
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Classification name
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Medical specialty
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Review panel
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Device class
2
Clearance type
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Statement or summary
Summary
Third party reviewed
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Applicant Contact#

Contact
Aaron Conovaloff
Address
1625 W. 3rd St. Tempe AZ US 85281 85281

FDA Registration Numbers#

Source Documents#

510(k) summary PDF